BEUDAMED
    39 results · 26ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    BIOSONIC SUVI PIEZEOELECTRIC SCALER AND POLISHER

    FDA 510(k)
    FDA Class 2 ·Dental

    ArgenZ ST 98x18 ML B2B

    FDA UDI
    ARGEN CORPORATION, THE·D818130137·Dental porcelain/ceramic restoration kit

    EVONOS

    FDA UDI
    Gyrus ACMI, LLC·00821925013308·LIPPY FOOTPLATE HOOK ANTERIOR,

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450189603·

    CONMED

    FDA UDI
    Conmed Corporation·10845854021347·OSCILLATING SAW BLADE 13 X 1.37 X 90 MM

    MClass

    FDA UDI
    Conmed Corporation·10845854020937·MClass Oscillating Saw Blade 1.37mm (0.054”) x ...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197045629·Adlerkreutz Tissue Forceps 2x3 te...

    N.A.

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011130137000·T separating disc, thickness 0.75 mm, ø 40 mm

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197045612·Adlerkreutz Tissue Forceps 2x3 te...

    COBAS 6000 C501 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JGS·May 7, 2009

    MEDTRONIC MINIMED SOF-SITE INFUSION SET, MODELS MMT-358S6, MMT-358M6, MMT-358L6, MMT-358S9, MMT-358M9, AND MMT-358L9

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SIDEKICK CIRCULAR FIXATOR SYSTEM: STRUTS AND HINGES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COBAS 6000 C501 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CEM·March 21, 2008

    T:SLIM X2 INSULIN PUMP WITH INTEROPERABLE TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·March 19, 2020

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·June 1, 2021

    COBAS 6000 C501MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·November 6, 2008

    ONYX

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·October 28, 2021

    POWERPACK

    FDA Adverse Event
    Malfunction ·ICC-NEXERGY·Product code IYN·September 3, 2013

    ONYX

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·October 28, 2021

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 6, 2016